Browsing by Author Cormand Rifà, Bru
Showing results 54 to 73 of 88
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| Issue Date | Title | Author(s) |
|---|---|---|
| 16-Aug-2018 | Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing | Corominas, Jordi; Klein, Marieke; Zayats, Tetyana; Rivero, Olga; Ziegler, Georg C.; Pauper, Marc; Neveling, Kornelia; Poelmans, Geert; Jansch, Charline; Svirin, Evgeniy; Geissler, Julia; Weber, Heike; Reif, Andreas; Arias Vasquez, Alejandro; Galesloot, Tessel E.; Kiemeney, Lambertus A. L. M.; Buitelaar, Jan K.; Ramos Quiroga, Josep Antoni; Cormand Rifà, Bru; Ribasés Haro, Marta; Hveem, Kristian; Gabrielsen, Maiken Elvestad; Hoffmann, Per; Jacob, Christian P.; Romanos, Marcel; Franke, Barbara; Lesch, Klaus-Peter |
| 8-Mar-2022 | Identification of genetic variants influencing methylation in brain with pleiotropic effects on psychiatric disorders. | Pineda-Cirera, Laura; Cabana Domínguez, Judit; Lee, Phil H.; Fernàndez Castillo, Noèlia; Cormand Rifà, Bru |
| 26-Sep-2022 | Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups | Mattheisen, Manuel; Grove, Jakob; Als, Thomas D.; Martin, Joanna; Voloudakis, Georgios; Meier, Sandra; Demontis, Ditte; Bendl, Jaroslav; Walters, Raymond; Carrey, Caitlin E.; Rosengren, Anders; Strom, Nora I.; Hauberg, Mads Engel; Zeng, Biao; Hoffman, Gabriel; Bybjerg-Grauholm, J.; Bækvad-Hansen, M.; Agerbo, Esben; Cormand Rifà, Bru; Nordentoft, Merete; Werge, Thomas; Mors, Ole; Hougaard, David M.; Buxbaum, Joseph D.; Faraone, Stephen V.; Franke, Barbara; Dalsgaard, Søren; Mortensen, Preben B.; Robinson, Elise B.; Roussos, Panos; Neale, Benjamin M.; Daly, Mark J.; Børglum, Anders D. |
| 1-Sep-2020 | Improved diagnosis of rare disease patients through systematic detection of runs of homozygosity | Matalonga Borrel, Lesley; Laurie, Steven; Papakonstantinou, Anastasios; Piscia, Davide; Mereu, Elisabetta; Bullich, Gemma; Thompson, Rachel; Horvath, Rita; Pérez Jurado, Luis; Riess, Olaf; Gut, Ivo; van Ommen, Gert Jan; Lochmüller, Hanns; Beltrán, Sergi; RD-Connect Genome-Phenome Analysis Platform and UR; Cormand Rifà, Bru; Balcells Comas, Susana; Grinberg Vaisman, Daniel Raúl; Urreizti, Roser; Garrabou Tornos, Glòria |
| 10-Nov-2020 | Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome | De Nittis, Pasquelena; Efthymiou. Sephanie; Sarre, Alexandre; Guex, Nicolas; Chrast, Jacqueline; Putoux, Audrey; Sultan, Tipu; Raza Alvi, Javeria; Ur Rahman, Zia; Zafar, Faisal; Rana, Nuzhat; Rahman, Fatima; Anwar, Najwa; Maqbool, Shazia; Zaki, Maha S.; Gleeson, Joseph G; Murphy, David; Galehdari, Hamid; Shariati, Gholamreza; Mazaheri, Neda; Sedaghat, Alireza; Lesca, Gaetan; Chatron, Nicolas; Salpietro, Vincenzo; Christoforou, Marilena; Houlden, Henry; Simonds, William F; Pedrazzini, Thierry; Maroofian, Reza; Reymond, Alexandre; Cormand Rifà, Bru; SYNAPS Study Group |
| 30-Jan-2018 | Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder | Pagerols Teixidó, Mireia; Richarte, Vanesa; Sánchez Mora, Cristina; Rovira, Paula; Soler Artigas, María; Garcia-Martínez, Iris; Calvo-Sánchez, Eva; Corrales, Montserrat; Santos da Silva, Bruna; Roth-Mota, Nina; Victor, Marcelo Moraes; Rohde, Luis Augusto; Grevet, Eugenio Horacio; Bau, Claiton Henrique Dotto; Cormand Rifà, Bru; Casas, Miquel; Ramos Quiroga, Josep Antoni; Ribasés Haro, Marta |
| 13-Jun-2020 | Involvement of the 14-3-3 gene family in autism spectrum disorder and schizophrenia: Genetics, transcriptomics and functional analyses | Torrico Avilés, Bàrbara; Antón Galindo, Ester; Fernàndez Castillo, Noèlia; Rojo Francàs, Eva; Ghorbani, Sadaf; Pineda Cirera, Laura; Hervás, Amaia; Rueda, Isabel; Moreno Guillén, Estefanía; Fullerton, Janice M.; Casadó, Vicent; Buitelaar, Jan K.; Rommelse, Nanda; Franke, Barbara; Reif, Andreas; Chiocchetti, Andreas G.; Freitag, Christine; Kleppe, Rune; Haavik, Jan; Toma, Claudio; Cormand Rifà, Bru |
| 5-Sep-2018 | Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan | Franke, Barbara; Michelini, Giorgia; Asherson, Philip; Banaschewski, Tobias; Bilbow, Andrea; Buitelaar, Jan K.; Cormand Rifà, Bru; Faraone, Stephen V.; Ginsberg, Yiva; Haavik, Jan; Kuntsi, Jonna; Larsson, Henrik; Lesch, Klaus-Peter; Ramos-Quiroga, J. Antoni; Réthelyi, János M.; Ribasés Haro, Marta; Reif, Andreas |
| Aug-2016 | Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine | International Headache Genetics Consortium; Cormand Rifà, Bru; Sintas Vives, Cèlia |
| 13-Sep-2017 | Metodologies d'alt rendiment per a la identificació de noves mutacions i gens causants de distròfies de retina: estudi funcional de nous candidats | Castro Miró, Marta de |
| 28-Mar-2022 | MicroRNA signatures associated with vulnerability to food addiction in mice and humans | García-Blanco, Alejandra; Domingo-Rodriguez, Laura; Cabana Domínguez, Judit; Fernàndez Castillo, Noèlia; Pineda-Cirera, Laura; Mayneris-Perxachs, Jordi; Burokas, Aurelijus; Espinosa-Carrasco, Jose; Arboleya, Silvia A; Latorre, Jessica; Stanton, Catherine; Cormand Rifà, Bru; Fernández-Real, Jose-Manuel; Martín-García, Elena; Maldonado, Rafael |
| 27-Jan-2023 | Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study | Welander, Nike Zoe; Rukh, Gull; Rask-Andersen, Mathias; Harder, Aster V.E.; The International Headache Genetics Consortium; van den Maagdenberg, Arn M.J.M.; Schiöth, Helgi Birgir; Mwinyi, Jessica; Cormand Rifà, Bru |
| 30-Aug-2018 | MIR-9, miR-153 and miR-124 are down-regulated by acute exposure to cocaine in adopaminergic cell model and may contribute to cocaine dependence | Cabana Domínguez, Judit; Arenas Solà, Concepción; Cormand Rifà, Bru; Fernàndez Castillo, Noèlia |
| 27-Aug-2021 | Molecular genetics of cocaine use disorders in humans | Fernàndez Castillo, Noèlia; Cabana Domínguez, Judit; Corominas Castiñeira, Roser; Cormand Rifà, Bru |
| 31-May-2017 | Mutation spectrum in the CACNA1A gene in 49 patients with episodic ataxia | Sintas Vives, Cèlia; Carreño, Oriel; Fernàndez Castillo, Noèlia; Corominas Castiñeira, Roser; Vila Pueyo, Marta; Toma, Claudio; Cuenca León, Ester; Barroeta, Isabel; Roig i Arnall, Carles; Volpini Bertrán, Víctor; Macaya Ruiz, Alfons; Cormand Rifà, Bru |
| 23-Jun-2021 | New Distance-Based approach for Genome-Wide Association Studies | Irigoien, I.; Cormand Rifà, Bru; Soler Artigas, María; Sánchez Mora, Cristina; Ramos-Quiroga, J.A.; Arenas Solà, Concepción |
| Jan-2022 | Non-mental diseases associated with ADHD across the lifespan: Fidgety Philipp and Pippi Longstocking at risk of multimorbidity? | Kittel-Schneider, Sarah; Arteaga-Henriquez, Gara; Arias Vasquez, Alejandro; Asherson, Phil; Banaschewski, Tobias; Brikell, Isabell; Buitelaar, Jan; Cormand Rifà, Bru; Faraone, Stephen V.; Freitag, Christine M.; Ginsberg, Ylva; Haavik, Jan; Hartman, Catharina A.; Kuntsi, Jonna; Larsson, Henrik; Matura, Silke; McNeill, Rhiannon V.; Ramos-Quiroga, J.Antoni; Ribasés Haro, Marta; Romanos, Marcel; Vainieri, Isabella; Franke, Barbara; Reif, Andreas |
| 22-Dec-2016 | Novel candidate genes and a wide spetrum of structural and point mutations responsible for inherited retinal dystrophies revealed by exome sequencing | Castro Miró, Marta de; Tonda, Raul; Escudero Ferruz, Paula; Andrés, Rosa; Mayor Lorenzo, Andres; Castro, Joaquín; Ciccioli, Marcela; Hidalgo, Daniel A.; Rodríguez Ezcurra, Juan José; Farrando, Jorge; Pérez Santonja, Juan J.; Cormand Rifà, Bru; Marfany i Nadal, Gemma; Gonzàlez-Duarte, Roser |
| 13-Feb-2017 | Nueva generación de biomarcadores epigenéticos y transcriptómicos en el cáncer de tiroides bien diferenciado | Buj Gómez, Raquel |
| 1999 | Patologia molecular de la malaltia de Gaucher | Grinberg Vaisman, Daniel Raúl; Cormand Rifà, Bru; Gort i Mas, Laura; Montfort Roca, Magda; Chabás Bergón, Amparo; Vilageliu i Arqués, Lluïsa |